PbS nanocrystal-doped SiO2 glass thin films and a single evaporated PbS fil
m were studied by X-ray photoelectron spectroscopy (XPS) and factor analysi
s (FA). The composite films contained PbS crystallites with mean dimensions
as small as 1-2 nm dielectrically embedded in the SiO2 host. Carrying out
XPS measurements, film compositions, charging, chemical bonding and size-re
lated effects were investigated. Electrostatic charging was observed in the
composite films decreasing opposite to the PbS content and was corrected u
sing the Si2p peak energy of SiO2 as an internal standard. With decreasing
mean crystallite size the valence band edge is shifted in correspondence to
the optical bandgap energies of the samples. In addition, peak shifts of s
ulphur and lead core levels are observed and evaluated by FA. From the anal
ysis of the S2s spectra, a spectrum of a surface like species is extracted
being 1.8 eV shifted in peak position to the PbS bulk line. Although some o
xygen is bonded to the lead atoms Pb-S-O compounds can be excluded by FA of
concatenated spectra. As the samples were ex situ prepared their surfaces
had to be sputter cleaned before the XPS investigations. Studying sputterin
g effects in XPS profile spectra we found out that Pb-S bonding can be cons
idered as resisting sputtering with the crystallites while the Pb-O bonding
is less stable under our sputtering conditions. (C) 1999 Elsevier Science
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